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Study of APG-2575 as a Single Agent or in Combination With Other Therapeutic Agents for CLL/SLL

PHASE1RECRUITING

Assess the safety and tolerability, identify dose-limiting toxicities (DLT) and determine the maximum tolerated dose (MTD) / recommended phase 2 dose (RP2D) of APG-2575.

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Study details:

The study will be conducted in two (2) parts and each part will consist of a ramp-up period, dose escalation and dose expansion portions. The duration of the ramp-up period will depend on the dose schedule being tested and will be conducted for both monotherapy and combination therapy. The ramp-up will consist of treatment with APG-2575 given once a day starting at 20 mg on Day 1, 50 mg on Day 2, 100 mg on Day 3, 200 mg on Day 4, 400 mg on Day 5¸ 600 mg on Day 6, 800 mg on Day 7, 1000 mg on Day 8 and 1200 mg on Day 9.

Scheduled maximum cohort doses for evaluation will start at 200 mg of APG-2575 to a maximum of 1200 mg of APG-2575. Consequently, patients with a scheduled maximum dose of 200 mg will have a 3-day ramp-up period, those scheduled at 400 mg, a 4-day ramp-up, and those scheduled at 600 mg, a 5-day ramp-up, etc, see Figure 1. Part 1 will study APG-2575 at different dose levels as monotherapy using a 3+3 dose escalation design with dose expansion at RP2D.

Part 2 will be combination of APG-2575 with rituximab or acalabrutinib or voruciclib Part 2 will be a 3+3 dose escalation of combination APG-2575 plus rituximab or acalabrutinib or voruciclib. Expansion cohorts at RP2D for the respective combinations will be conducted to further evaluate safety and anticancer activity.

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Eligibility criteria

Researchers look for people who fit a certain description, called eligibility criteria. See if you qualify.

Inclusion criteria

≥18 years of age.

Histologically confirmed chronic lymphocytic leukemia (CLL) or small lymphocytic leukemia (SLL) according to the 2018 international workshop (IW) CLL criteria who must have relapsed or be refractory to at least one prior therapy for CLL/SLL and require treatment by 2018 IWCLL criteria.

ECOG) ≤2.

Patient must have objectively documented evidence of disease progression prior to study entry such as: escalating lymphocytes count with an increase > 50% over a period of two months or doubling time in less than 6 months; enlarging adenopathy or splenomegaly; increasing cytopenias; clinical B symptoms -night sweats, fatigue, > 1% weight loss in 6 months, fevers > 100.50F for ≥ one month without infection.

In Part 1 of the APG-2575 monotherapy dose escalation portion, patients eligible for dose expansion at doses lower than MTD will have received ≤ 3 prior systemic lines of therapy.

Adequate bone marrow function independent of growth factor: Absolute neutrophil count (ANC)≥1.0× 109/L in patient without bone marrow involvement. This criterion does not apply to patients with bone marrow involvement by CLL/SLL. Platelets count ≥30 x 109/L (entry platelet count must be independent of transfusion within 7 days of first dose of study drug).

Adequate renal and hepatic function as indicated by: Serum creatinine ≤1.5×upper limit of normal (ULN); if serum creatinine is >1.5×ULN, creatinine clearance must be ≥ 50 mL/min, calculated using the Cockcroft and Gault formula(140-Age)x mas (kg)/(72x creatinine mg/dL); multiply by 0.85 if female (Cockcroft 1976) Total bilirubin ≤1.5 x ULN, except patients with known Gilbert's syndrome. Aspartate aminotransferase (AST) and Alanine aminotransferase (ALT) <2.5 x ULN, Alkaline phosphatase<2.5×ULN International normalized Ratio (INR), Prothrombin Time (PT) or Activated Partial Thromboplastin time (APTT)≤1.5×ULN unless the patient is receiving anticoagulant therapy as long as PT or APTT is within therapeutic range of intended use of anticoagulants.

Females of childbearing potential (i.e. not postmenopausal for at least 2 years or surgically sterile) must have negative results for pregnancy test performed: At Screening on a serum sample obtained within 14 days prior to the first study drug administration Prior to dosing on a urine sample obtained on the first day of study drug administration, if it has been >7 days since obtaining the serum pregnancy test results.

Females of childbearing potential and non-sterile males must practice at least one of the following methods of birth control with partner(s) throughout the study and for 90 days after discontinuing study drug: Total abstinence from sexual intercourse as the preferred lifestyle of the patient; periodic abstinence is not acceptable; Surgically sterile partner(s); acceptable sterility surgeries are: vasectomy, bilateral tubal ligation, bilateral oophorectomy or hysterectomy; Intrauterine device (IUD); Double-barrier method (contraceptive sponge, diaphragm or cervical cap with spermicidal fellies or cream AND a condom); Hormonal contraceptives (oral, parenteral, vaginal ring or transdermal) for at least 3 months prior to study drug administration. If hormonal contraceptives are used, the specific contraceptive must have been used for at least 3 months prior to study drug administration.

Male patients must refrain from sperm donation, from initial study drug administration until 90 days after the last dose of study drug.

Ability to understand and willingness to sign a written informed consent form (the consent form must be signed by the patient prior to any study-specific procedures).

Willingness and ability to comply with study procedures and follow-up examination.

Exclusion criteria

Patient has undergone allogeneic stem cell transplant < 90 days

Patient has active graft-versus-host disease or require immunosuppressive therapy.

Richter's Syndrome.

Prior anti-Bcl-2 treatment (except patients who discontinued treatment for reasons other than disease progression)

For combination cohorts: In the acalabrutinib and APG-2575 cohort, patients who are on anticoagulants or patients that discontinued due to acalabrutinib toxicity (Note: Patients who received a BTK inhibitor therapy may participate whether, or not, they progressed following BTK inhibitor treatment). Prior CDK-9 inhibitor in the voruciclib plus APG-2575 cohort

Known human immunodeficiency virus syndrome (HIV) infection

Known active hepatitis B infection, as defined seropositivity for Hep B surface antigen (HBsAg) or known hepatitis C infection as determined by hepatitis C antibody with elevated liver enzymes as defined in the inclusion criteria or any other evidence of active hepatitis C such as currently on treatment

Has known central nervous system (CNS) involvement.

Prior malignancy that required treatment and has shown recurrence within 2 years of screening (except for non-melanoma skin cancer or adequately treated carcinoma in situ of cervix or breast). Cancer treated within 2 years with curative intent and without recurrence as well as prostate cancer on active surveillance are allowed.

Concurrent treatment with an investigational agent, received biologics (≤28 days), or small molecule targeted therapies (≤5 half-life) or other anti-cancer therapies (including chemotherapy) ≤14 days of first dose of study drug

Patient is pregnant or breast feeding

Has received the following within 7 days prior to the first dose of study drug: Steroid therapy at a dose greater than prednisone 20 mg daily (or equivalent) for anti-neoplastic intent; CYP3A inhibitors such as fluconazole, ketoconazole, and clarithromycin; Potent CYP3A inducers such as rifampin, carbamazepine, phenytoin, and St. John's wort;

Radiation within 14 days of study entry

Continuance of toxicities due to prior radiotherapy or chemotherapy agents that have not recovered to ≤ grade 1 or baseline, except alopecia or neuropathy.

Failure to recover adequately, as judged by the investigator, from prior surgical procedures. Patient with active wound healing, patients who have had major surgery within 28 days from 1st dose of study drug

Has a cardiovascular disability status of New York Heart Association Class ≥ 2. Class 2 is defined as cardiac disease in which patients are comfortable at rest but ordinary physical activity results in fatigue, palpitations, dyspnea or anginal pain.

Unstable angina or myocardial infarction within 3 months of enrollment

QTc interval> 480ms (Bazett or Fredericia formulae) or other remarkable abnormal ECG findings, including second-degree type II atrioventricular block, third-degree atrioventricular block or bradycardia (ventricular rate of less than 50 beats per minute).

Has gastrointestinal conditions that could affect the absorption of APG-2575 in the opinion of the Investigator.

Uncontrolled concurrent illness including, but not limited to: uncontrolled diabetes mellitus, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with the study requirements.

Any other condition or circumstance that would, in the opinion of the investigator, make the patient unsuitable for participation in the study.

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Eligibility

Age eligible for study : 18 and older

Healthy volunteers accepted : No

Gender eligible for study: All

Things to know

Study dates

Study start: 2020-03-02

Primary completion: 2025-03-30

Study completion finish: 2026-06-30

Study type

TREATMENT

Phase

PHASE1

Trial ID

NCT04215809

Intervention or treatment

DRUG: APG2575

Conditions

• CLL/SLL

Condition: CLL/SLL
DRUG: APG2575
Brisbane, Queensland, Australia and more
Sponsor: Ascentage Pharma Group Inc.

You may be eligible to participate in this trial based on your search. Check eligibility by answering some questions.

Are you running this trial? If you're a clinic or sponsor, you can claim this study. Claim or learn more.

Find a site

Closest Location:

Princess Alexandria Hospital

Research sites nearby

Select from list below to view details:

Princess Alexandria Hospital
Brisbane, Queensland, Australia
Frankston Private Hospital
Melbourne, Victoria, Australia

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Participant Group/Arm	Intervention/Treatment
EXPERIMENTAL: APG2575 200mg APG2575 200mg ramp up	DRUG: APG2575 APG2575 investigation drug in ramp up dosing
EXPERIMENTAL: APG2575 400mg APG2575 400mg ramp up	DRUG: APG2575 APG2575 investigation drug in ramp up dosing
EXPERIMENTAL: APG 2575 600mg APG2575 600mg ramp up	DRUG: APG2575 APG2575 investigation drug in ramp up dosing
EXPERIMENTAL: APG2575 800mg APG2575 800mg ramp up	DRUG: APG2575 APG2575 investigation drug in ramp up dosing
EXPERIMENTAL: APG2575 1000 mg APG2575 1000 mg ramp up	DRUG: APG2575 APG2575 investigation drug in ramp up dosing
EXPERIMENTAL: APG2575 1200mg APG2575 1200mg ramp up	DRUG: APG2575 APG2575 investigation drug in ramp up dosing

What is the study measuring?

Primary outcome

Primary Outcome Measure	Primary Outcome Description	Primary Outcome Time Frame
Primary Toxicity Endpoint: dose limiting toxicity (DLT)	DLT will be defined based on the rate of drug-related grade 3-5 adverse events experienced within the first 6 weeks (2 cycles) of study treatment. These will be assessed via CTCAE version 5.0	42 days
Maximally tolerated dose (MTD)	MTD will be determined based on DLTs observed during the first 6 weeks (2 cycles) of study treatment	42 days

Secondary outcome

Frequently Asked Questions

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References

Clinical Trials Gov: Study of APG-2575 as a Single Agent or in Combination With Other Therapeutic Agents for CLL/SLL